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2017 | 56 | 3 | 149-160

Article title

Cortical Localization of α- and γ-Tubulin and the Assembly of Cortical Microtubule Cytoskeleton in Hypotrichous Ciliate Euplotes eurystomus

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Abstracts

EN
This study aimed to investigate the assembly characteristics of ciliature and cortical microtubules and the localization of tubulins in different depths and regions of the cortex. The hypotrichous ciliates have closely arranged cilia and a highly complex microtubular system. Direct fluorescence and immunofluorescence labeling were used to observe ciliary organelles and cortical microtubular cytoskeleton in Euplotes eurystomus. An immunofluorescence analysis demonstrated that α-tubulin localized to the ventral and dorsal ciliary organelles and their associated microtubules, while γ-tubulin localized to the basal bodies of ciliary organelles, macronuclear membrane, and excretory pore of a contractile vacuole in the interphase. A direct fluorescence analysis showed that the ciliature and cortical microtubules in the deep cortex were more clearly marked by fluorescent taxoid (FLUTAX). Interestingly, α- and γ-tubulins also colocalized to the ringlike ciliary base–associated microtubules of dorsal kineties. The short microtubular bundles between the bases of transverse cirri could be marked by FLUTAX and γ-tubulin rather than α-tubulin, suggesting that tubulins in cortical microtubules in E. eurystomus varied, and the differentiation of cortical microtubules in the hypotrichous ciliate tended to be versatile. Also, during morphogenesis, γ-tubulin also localized to the base of ciliary primordium, where new basal bodies were formed, suggesting that the endocellular position of γ-tubulin in ciliates was related to basal bodies and regulated by the cell cycle. This study might help understand the assembly characteristics and tubulin composition of microtubules in different depths and regions of the cortex in hypotrichous ciliate E. eurystomus.

Year

Volume

56

Issue

3

Pages

149-160

Physical description

Dates

published
2017

Contributors

author
  • Department of Biochemistry, Zunyi Medical University, Zunyi, Guizhou, China
  • School of Life Science, East China Normal University, Shanghai, China
author
  • Laboratory of Basic Medical Morphology, Zunyi Medical University, Zunyi, Guizhou, China
author
  • Department of Biochemistry, Zunyi Medical University, Zunyi, Guizhou, China
author
  • Department of Biochemistry, Zunyi Medical University, Zunyi, Guizhou, China

References

  • Allen R. D. (1967) Fine structure, reconstruction and possible fuctions of components of the cortex of Tetrahymena pyriformis. J. Eukaryot. Microbiol. 14: 553–565
  • Allen R. D. (1969) The morphogenesis of basal bodies and accessory structure of the cortex of the ciliated protozoan Tetrahymena pyriformis. J. Cell Biol. 40: 716–733
  • Arregui L., Muñoz-Fontela C., Serrano S., Barasoain I., Guinea A. (2002) Direct visualization of the microtubular cytoskeleton of ciliate protozoa with a fluorescent taxoid. J. Eukaryot. Microbiol. 49: 312–318
  • Beisson J., Wright M. (2003) Basal body/centriole assembly and continuity. Curr. Opin. Cell Biol. 15: 96–104
  • Binarová P., Cenklová V., Hause B., Kubátová E., Lysák M., Dolezel J., Bögre L., Dráber P. (2000) Nuclear gamma-tubulin during acentriolar plant mitosis. Plant Cell12: 433–442
  • Díaz J. F., Strobe R., Engelborghs Y., Souto A. A., Andreu J. M. (2000) Molecular recognition of Taxol by microtubules: Kinetics and thermodynamics of binding of Fluorescent Taxol derivatives to an exprosed site. J. Biol. Chem. 275: 265–276
  • Elmendorf G. H., Dawson C. S., McCaffery M. J. (2003) The cytoskeleton of Giardia lamblia. Int. J. Parasitol. 33: 3–28
  • Evangelio J. A., Abal M., Barasoain I., Souto A. A., Lillo M. P., Acuña A. U., Amat-Guerri F., Andreu J. M. (1998) Fluorescent taxoids as probes of the microtubule cytoskeleton. Cytoskeleton39: 73–90
  • Fuller S. D., Gowen B. E., Reinsch S., Sawyer A., Buendia B., Wepf R., Karsenti E. (1995) The core of the mammalian centriole contains gamma-tubulin. Curr. Biol. 5: 1384–1393
  • Gaeritg J. (2000) Molecular mechanisms of microtubular organelle assembly in Tetrahymena.J. Eukaryot. Microbiol. 47: 185–190
  • Gu F. K. (1991) Introduction to protozoology. Higher Education Press, Peking.
  • Gu F. K., Zou S. F., Li Y. S., Ni B. (2003) Scanning electron microscopic observations on the ventral cortical cytoskeleton of Euplotes harpa (Protozoa, Ciliophora). Acta Zool. Sinica 49: 514–521
  • Iftode F., Clérot J. C., Levilliers N., Bré M. H. (2000) Tubulin polyglycylation: a morphogenetic marker in ciliates. Biol. Cell 92: 615–628
  • Iftode F., Fleury-Aubusson A. (2003) Structural inheritance in Paramecium: ultrastructural evidence for basal body and associated rootlets polarity transmission through binary fission. Biol. Cell 95: 39–51
  • Kilburn C. L., Pearson C. G., Romijn P. E., Meehl J. B., Giddings T. H., Culver B. P., Yates J. R., Winey M. (2007) New Tetrahymena basal body protein components identify basal body domain structure. J. Cell Biol. 178: 905–912
  • Klotz C., Ruiz F., Loubresse N. G. D., Wright M., Dupuid-Williams P., Beisson J. (2003) Gamma-tubulin and MTOCs in Paramecium. Protist 154: 193–209
  • Kovács P., Csaba G., Pállinger É., Czaker R. (2007) Effects of taxol treatment on the microtubular system and mitochondria of Tetrahymena. Cell Biol. Int. 31: 724–732
  • Lajoie-Mazenc I., Tollon Y., Detraves C., Julian M., Moisand A., Gueth-Hallonet C., Debec A., Salles-Passador I., Puget A., Mazarguil H. (1994) Recruitment of antigenic gamma-tubulin during mitosis in animal cells: presence of gamma-tubulin in the mitotic spindle. J. Cell Sci. 107: 2825–2837
  • Lechtreck F. K., Geimer S. (2000) Distribution of polyglutamylated tubulin in the flagellar apparatus of green flagellates. Cell Motil. Cytoskel. 47: 219–235
  • Liang A., Heckmann K. (1993) The macronuclear γ-tubulin-encoding gene of Euplotes octocarinatus contains two introns and an in-frame TGA. Gene136: 319–322
  • Liang A., Ruiz F., Heckmann K., Klotz C., Tollon Y., Beisson J., Wright M. (1996) Gamma-tubulin is permanently associated with basal bodies in ciliates. Eur. J. Cell Biol. 70: 331–338
  • Libusová L., Dráber P. (2006) Mutiple tubulin forms in ciliated protozoan Tetrymena and Paramecium species. Protoplasma227: 65–76
  • Lou H. L., Gao W., Ni B., Gu F. K. (2007) Morphology and morphogenesis of the ciliature microtubular organelles in the ventral cortex of Paraurostyla weissei (Hyportrichida, Ciliophora). Acta Zool. Sinica 53: 742–749
  • Loubresse N. G. D., Riuz F., Beisson J., Klotz C. (2001) Role of delta-tubulin and the C-tubule in assembly of Paramecium basal bodies. BMC Cell Biol. 2: 1–7
  • Lynn D., Small E. B. (1981) Protist kinetids: Structual conservatism, kinetid structure, and ancestral states. Biosystems14: 377–385
  • Marshall W. F., Rosenbaum J. L. (2003) Tubulin superfamily – Giving Birth to Triplets. Curr. Biol. 13: R55–R56
  • Marziale F., Pucciarelli S., Ballarini P.,Melki R., Uzun A., Llyin V. A., Detrich H. W., Miceli C. (2008) Different roles of two γ-tubulin isotypes in the cytoskeleton of the Antarctic ciliate Euplotes focardii: Remodelling of interaction surfaces may enhance microtubule nucleation at low temperature. FEBS J. 275: 5367–5382
  • Moritz M., Braunfeld M. B., Sedat J. W., Alberts B., Agard D. A. (1995) Microtubule nucleation by γ-tubulin-containing rings in the centrosome. Nature378: 638–640
  • Oakley C. E., Oakley B. R. (1989) Identification of a γ-tubulin, a new member of the tubulin superfamily encoded by mipA gene of Aspergillus nidulans. Nature338: 662–664
  • Olins D. E., Olins A. L., Robert-Nicoud M., Jovin T. M., Wehland J., Weber K. (1989) Differential distribution of α-tubulin isotypes in E. eurystomus determined by confocal immunofluorescence microscopy. Biol. Cell66: 235–246
  • Oz S., Ivashkopachima Y., Gozes I. (2012). The ADNP derived peptide, NAP modulates the tubulin pool: implication for neurotrophic and neuroprotective activities. PloS One7: 1411–1411
  • Ruiz F., Beisson J., Rossier J., Dupuis-Williams P. (1999) Basal body duplication in Paramecium requires γ-tubulin. Curr. Biol. 9: 43–46
  • Sambrook J., Fritsch F., Maniatis T. (1992) Molecular Clone: a Laboratory Manual. Cold Spring Harbor Laboratory Press, New York, NY.
  • Scott V., Sherwin T., Gull K. (1997) Gamma-tubulin in Trypanosomes: Molecular characterization and location to multiple and diverse microtubule organizing centres. J. Cell Sci. 110: 157–168
  • Shang Y. H., Li B., Gorovsky M. A. (2002) Tetrahymena thermophila contains a conventional γ-tubulin that is differentially required for the maintenance of different microtubule-organizing centers. J. Cell Biol. 158: 1195–1206
  • Sheng X., Zeng H., Zhang M., Yun M. X., Yin F., Gu F. K. (2011) Influences of the interference of the γ-tubulin gene expression on the morphology and microtubules of ciliate E. eurystomus. Zool. Sci. 28: 476–481
  • Shu H. B., Li Z., Palacios M. J., Li Q., Joshi H. C. (1995) A transient associated of gamma-tubulin at the midbody is required for the completion of cytokinesis during the mammaliam-cell division. J. Cell Sci. 108: 2955–2962
  • Tan M., Heckmann K. (1998) The two γ-tubulin-encoding genes of the ciliate Euplotes crassus differ in their sequences, codon usage, transcription initiation sites and poly (A) addition sites. Gene210: 53–60
  • Zhou S. J., Yin F., Sheng X., Gu F. K. (2008) Morphology and morphogenesis of the ciliature microtubular organelles in the ventral cortex of Pseudourostyla cristata (Hyportrichida , Ciliophora). Acta Zool. Sinica54: 299–308
  • Zhu H. (1984) The contractile vacuole. Bull Biol. 4: 3–5

Document Type

Publication order reference

Identifiers

Biblioteka Nauki
52393951

YADDA identifier

bwmeta1.element.ojs-doi-10_4467_16890027AP_17_013_7494
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